Evidence map›Paper›PMID 11345439›Full record

ArticleRNA (New York, N.Y.)2001

A selection system for identifying accessible sites in target RNAs.

W H Pan, H F Devlin, C Kelley, H C Isom, G A Clawson

Abstract read
In one paragraph

Article in RNA (New York, N.Y.), 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

  1. Article
  2. MicroRNAs align with accessible sites in target mRNAs.Journal of cellular biochemistry · 2010
    Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

W H PanDepartment of Pathology, Biochemistry and Molecular Biology, The Gittlen Cancer Research Institute, The Pennsylvania State University, Hershey 17033, USA.
H F Devlin
C Kelley
H C Isom
G A Clawson

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although ribozymes offer tremendous potential for posttranscriptionally controlling expression of targeted genes, their utility is often limited by the accessibility of the targeted regions within the RNA transcripts. Here we describe a method that identifies RNA regions that are accessible to oligonucleotides. Based on this selection protocol, we show that construction of hammerhead ribozymes targeted to the identified regions results in catalytic activities that are consistently and substantially greater than those of ribozymes designed on the basis of computer modeling. Identification of accessible sites should also be widely applicable to design of antisense oligonucleotides and DNAzymes.

Indexed as

RNA, CatalyticBase SequenceDirected Molecular EvolutionDNA, CatalyticHepatitis B virusModels, MolecularMolecular Sequence DataNucleic Acid ConformationOligonucleotides, AntisenseRNA Processing, Post-TranscriptionalRNA, Small UntranslatedRNA, ViralSubstrate SpecificityDNA, CatalyticOligonucleotides, AntisenseRNA, CatalyticRNA, Small UntranslatedRNA, Viral

Identifiers

PMID11345439
PMCPMC1370114

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.